Quality Consultant - QMS responsible
Technolution
Details, standards, procedures, writing, and more details – are you ready to be the owner of our QMS?
As our QMS responsible, with at least 5 years of experience, you know your way around Pharma or MedTech standards, and you take pride in knowing every corner of the QMS.
Don’t be careful what you wish for
Because we are quite confident to be able to grant all your wishes. You will be part of a small and highly experienced Quality Management-team, and you will have an important, split role. First of all, you will be working with our clients facilitating efficient quality management within the Medical Device industry, specifically IVD and Combination Products.
Besides that, you are going to upgrade our own QMS and help the process owners in Technolution. We work together, and there is always help and sparring within close range, if you should need it. As a consultant, you will work on diverse projects with start-ups to industry leaders, some days from the office in Hørsholm, some days onsite at the clients and some days remote. And by the way: being a consultant is not equivalent to being a lone wolf: you will always be part of a team.
We have a few wishes too
You have a minimum of 5 years of experience working with Quality Management in Pharma or MedTech, you have an intuitive understanding of how standards play out and how to apply them. You are very familiar with standards such as ISO 13485, EU and FDA regulations for MD, IVD and Combination Products. You find it natural to build good relations with clients and colleagues, because you probably already experienced that this approach creates the best results.
If you are ready to take ownership of our QMS, then join us at Technolution, where your experience and skills will make a significant impact!
Department: Quality Management & Regulatory
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